Canonical Allele Identifier: CA403989188

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464894A>G (hg19) ; chr19:g.10354218A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354218A>G , CM000681.2:g.10354218A>G	GRCh38
NC_000019.9:g.10464894A>G , CM000681.1:g.10464894A>G	GRCh37
NC_000019.8:g.10325894A>G	NCBI36
NG_007872.1:g.31355T>C , LRG_121:g.31355T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1081T>C	ENSP00000514307.1:n.*1081T>C
ENST00000525976.6:c.2732T>C	ENSP00000434831.2:p.Val911Ala
ENST00000527481.3:c.2732T>C	ENSP00000466340.2:p.Val911Ala
ENST00000529370.6:n.4108T>C
ENST00000529739.2:n.3146T>C
ENST00000530829.2:c.*2283T>C	ENSP00000436826.2:n.*2283T>C
ENST00000531836.6:c.2732T>C	ENSP00000436175.2:p.Val911Ala
ENST00000533334.2:c.*774T>C	ENSP00000432320.2:n.*774T>C
ENST00000534228.2:n.4191T>C
ENST00000699354.1:n.834T>C
ENST00000699355.1:c.*1837T>C	ENSP00000514328.1:n.*1837T>C
ENST00000699356.1:n.3146T>C
ENST00000699357.1:n.4191T>C
ENST00000699358.1:c.2732T>C	ENSP00000514329.1:p.Val911Ala
ENST00000699360.1:c.2732T>C	ENSP00000514331.1:p.Val911Ala
ENST00000525621.6:c.2732T>C MANE Select	ENSP00000431885.1:p.Val911Ala
ENST00000264818.10:c.2732T>C	ENSP00000264818.6:p.Val911Ala
ENST00000524462.5:c.2177T>C	ENSP00000433203.1:p.Val726Ala
ENST00000525621.5:c.2732T>C	ENSP00000431885.1:p.Val911Ala
ENST00000527481.2:c.28T>C
ENST00000529412.1:n.404T>C
ENST00000530560.5:c.161T>C	ENSP00000465291.1:p.Val54Ala
NM_003331.4:c.2732T>C , LRG_121t1:c.2732T>C	NP_003322.3:p.Val911Ala
XM_011528245.1:c.2732T>C	XP_011526547.1:p.Val911Ala
XM_011528246.1:c.2435T>C	XP_011526548.1:p.Val812Ala
XM_011528247.1:c.2435T>C	XP_011526549.1:p.Val812Ala
XM_011528248.1:c.2732T>C	XP_011526550.1:p.Val911Ala
XM_011528249.1:c.1406T>C	XP_011526551.1:p.Val469Ala
XM_011528251.1:c.989T>C	XP_011526553.1:p.Val330Ala
XM_011528246.3:c.2435T>C	XP_011526548.1:p.Val812Ala
XM_011528249.2:c.1406T>C	XP_011526551.1:p.Val469Ala
XR_001753750.1:n.2889T>C
XR_001753751.1:n.2889T>C
XR_002958353.1:n.3815T>C
NM_003331.5:c.2732T>C MANE Select	NP_003322.3:p.Val911Ala
NM_001385197.1:c.2732T>C	NP_001372126.1:p.Val911Ala
NM_001385198.1:c.2732T>C	NP_001372127.1:p.Val911Ala
NM_001385199.1:c.2546T>C	NP_001372128.1:p.Val849Ala
NM_001385200.1:c.2729T>C	NP_001372129.1:p.Val910Ala
NM_001385201.1:c.2534T>C	NP_001372130.1:p.Val845Ala
NM_001385202.1:c.2648T>C	NP_001372131.1:p.Val883Ala
NM_001385203.1:c.2813T>C	NP_001372132.1:p.Val938Ala
NM_001385204.1:c.2942T>C	NP_001372133.1:p.Val981Ala
NM_001385205.1:c.2642T>C	NP_001372134.1:p.Val881Ala
NM_001385206.1:c.2606T>C	NP_001372135.1:p.Val869Ala
NM_001385207.1:c.2714T>C	NP_001372136.1:p.Val905Ala